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首页> 外文期刊>ACS Omega >Pharmacological Screening of Mangifera indica Seeds for Antidepressant-like Action Along with a Mechanistic Study
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Pharmacological Screening of Mangifera indica Seeds for Antidepressant-like Action Along with a Mechanistic Study

机译:Mangifera籼稻种子的药理筛选与机械研究的抗抑郁药动作

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Depression is emerging as a major global issue. There are several antidepressants available in the market, but their efficacy is usually unpredictable. Therefore, there is a need to find an alternative therapeutic agent with better therapeutic efficacy and availability. In the current investigation, the antidepressant-like action of the aqueous methanolic extract of Mangifera indica seeds (25, 50, and 100 mg/kg) was evaluated by two predictive models like the tail suspension test and forced swimming test along with the determination of the mechanism of action working behind this action. The results of the acute treatment with the extract show a dose-dependent reduction in the duration of immobility in both models. The antidepressant-like action of the extract (100 mg/kg) was blocked by the administration of p -chlorophenyl alanine, α-methyl-p -tyrosine, prazosin, and sulpiride while remaining unaffected with propranolol. In contrast, the administration of d-serine along with the extract (a full agonist of glycine/N -methyl-d-aspartate, NMDA, receptors) diminished the anti-immobility action. The administration of the extract along with nitro-l-arginine-methyl ester synergizes into the anti-immobility action of the extract, and intake of l-arginine remained unable to effect this action, whereas sildenafil blocks the effect. The antidepressant-like action of the extract is probably due to the involvement of serotonergic and adrenergic (mainly α receptors are involved) systems, an NMDA receptor complex, and the nitric oxide pathway.
机译:抑郁症是作为一个主要的全球问题。市场上有几种抗抑郁药,但它们的疗效通常是不可预测的。因此,需要寻找具有更好治疗功效和可用性的替代治疗剂。在目前的研究中,通过尾悬架试验和强制游泳测试等两个预测模型评价含水甲醇提取物的抗抑郁药物甲醇提取物的抗抑郁药物。确定该行动背后行动机制。用提取物的急性治疗结果显示出两种模型中不动的持续时间依赖性降低。提取物(100mg / kg)的抗抑郁药物通过给予对二氯苯基丙氨酸,α-甲基 - 1> p纯溶胶,普拉索汀和硫三胺而阻断,同时仍然不受丙醇溶胶的影响。相反,将D-丝氨酸与提取物(甘氨酸/ N-甲基-D-天冬氨酸N-甲基-D-天冬氨酸,NMDA,受体的全激动剂施用给药减少了抗移植作用。提取物与硝基-L-精氨酸 - 甲基酯的施用促进到提取物的抗分动作用中,并摄入L-精氨酸仍然不能影响该动作,而西地那非阻断了该效果。提取物的抗抑郁药作用可能是由于血清组织能和肾上腺素能(主要是α受体涉及)系统,NMDA受体复合物和一氧化氮通路的累积。

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